|
HS Code |
267675 |
| Product Name | 2,6-Dichloro-4-(Trifluoromethyl)Benzenesulfonyl Chloride |
| Cas Number | 2765-68-6 |
| Molecular Formula | C7H2Cl2F3O2S |
| Molecular Weight | 297.06 |
| Appearance | White to off-white solid |
| Melting Point | 60-64°C |
| Boiling Point | N/A (decomposes) |
| Density | 1.67 g/cm3 |
| Solubility | Reacts with water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=C(C=C(C(=C1Cl)S(=O)(=O)Cl)Cl)C(F)(F)F |
| Ec Number | 220-431-1 |
As an accredited 2,6-Dichloro-4-(Trifluoromethyl)Benzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 100-gram amber glass bottle, sealed tightly, with hazard labeling, and stored in a secondary protective container. |
| Shipping | 2,6-Dichloro-4-(Trifluoromethyl)Benzenesulfonyl Chloride is shipped in sealed, chemically resistant containers to prevent moisture and air exposure. Packages comply with hazardous material transport regulations, featuring proper labeling and documentation. Temperature-sensitive and handled with care, the shipment avoids direct sunlight and is securely packed to minimize breakage and leaks during transit. |
| Storage | Store **2,6-Dichloro-4-(Trifluoromethyl)benzenesulfonyl chloride** in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and direct sunlight. Keep it away from incompatible substances such as water, alcohols, bases, and strong oxidizers. Handle under an inert atmosphere if possible, and use appropriate personal protective equipment. Store in a corrosion-resistant container. |
Applications of 2,6-Dichloro-4-(Trifluoromethyl)Benzenesulfonyl Chloride in Industrial Manufacturing2,6-Dichloro-4-(Trifluoromethyl)Benzenesulfonyl Chloride serves as a key intermediate in specialty chemical syntheses. The following applications demonstrate established downstream segments where this compound plays an integral role in manufacturing, with process-specific compliance and technical requirements detailed for each sector. 1. Agrochemical Active Ingredient SynthesisProducers in the agrochemical industry utilize this sulfonyl chloride as a critical sulfonation agent during the synthesis of selective herbicide actives, particularly sulfonylurea-based products. The material introduces functional sulfonyl groups at advanced stages of API development, impacting bioactivity and selectivity. Formulation engineers closely control addition rates and temperature profiles to achieve consistent organoleptic and field performance in the end product. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical API Intermediate ManufacturingPharmaceutical manufacturers use this chemical as a sulfonylation and protecting group reagent during the synthesis of advanced pharmaceutical intermediates, especially those targeting CNS and anti-inflammatory small molecules. Careful adjustment of addition sequence and thermal conditions ensures site-specific sulfonation, minimizing impurities. The material must meet stringent purity and trace metal limits to comply with regulatory expectations for GMP environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronics Industry: Photoresist and Circuit Board IntermediateFabricators in the electronics sector deploy 2,6-Dichloro-4-(Trifluoromethyl)Benzenesulfonyl Chloride for producing sulfonated aromatic monomers, which serve as components in advanced photoresist polymers and copper-clad laminate matrices. The controlled introduction of the compound enhances etch resistance and adhesion properties. Purity profile and trace ionic contamination must meet electronics-grade requirements to prevent conductivity defects. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Polymer and Membrane ManufacturingThe specialty polymer sector incorporates this sulfonyl chloride derivative in the functionalization of aromatic polymers, especially sulfonated poly(arylene ether sulfone) membranes. These membranes find use in proton exchange membranes for fuel cells and separation devices. The material delivers high sulfonation degree and site fidelity, and adjustment of addition rate directly determines proton conductivity and physical stability in the resultant membrane. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,6-Dichloro-4-(Trifluoromethyl)Benzenesulfonyl Chloride prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
2,6-Dichloro-4-(trifluoromethyl)benzenesulfonyl chloride, often recognized by practitioners as a specialized aromatic sulfonyl chloride, brings robust reactivity and selectivity to synthesis applications. Over several years of hands-on production, several lessons have come through clearly. There is no substitute for careful control during chlorination and handling of the trifluoromethyl substitution, since these steps influence downstream behaviors and purity of the finished compound. This material, once completed, stands apart from simpler sulfonyl chlorides used in commodity-grade synthesis work.
Engineers on the shop floor regularly encounter these white-to-pale crystalline solids during the packing phase. The product emits a strong, characteristic odor that quickly signals its presence. In comparison to basic benzenesulfonyl chloride, its melting point range sits higher, which reflects the added structural complexity. Handling and transportation require airtight containers and careful personal protective equipment. Eye and skin protection, plus appropriate ventilation, cannot be compromised; the reactive nature of both sulfonyl chloride and the dichloro-trifluoromethyl structure mandates these measures.
Years at the plant have shown that research chemists and process development teams look for 2,6-dichloro-4-(trifluoromethyl)benzenesulfonyl chloride when designing advanced agrochemical and pharmaceutical molecules. Its strong electron-withdrawing groups (dichloro- and trifluoromethyl) enhance reactivity, which pushes it up the list for demanding sulfonylation reactions. Medicinal chemistry teams value how the bulk and polarity contribute to biological activity, sometimes unlocking molecules that would otherwise stall out in screening. Plant managers receive regular requests for custom volumes, from pilot-scale batches for process optimization up to multi-ton annual supply for commercialized molecules.
The nature of the raw materials and the chlorination stages introduces sensitivity not only to temperature control but also to residual moisture. As operators have learned, even small deviations can produce colored impurities or decrease final assay. In-situ generation of sulfonyl chlorides avoids unnecessary byproducts, but this demands rapid and skilled downstream workup. Automated dosing and continuous monitoring add a layer of reliability, but strict training is needed for technicians on both quality and safety. A manufacturer following reactive chemistry up close gains appreciation for the balance between precision and throughput: too slow and yields suffer, too fast and isolation purity falls off.
Direct experiences in synthesis highlight the difference between this compound and typical benzenesulfonyl chloride or the mono-chloro derivatives found in less demanding processes. The paired dichloro moieties plus trifluoromethyl substitution create an electron-deficient ring, which leads to higher reactivity than single halogen analogs. This can open new synthetic pathways, especially in constructing sulfonamide bonds where standard benzenesulfonyl chloride would deliver sluggish or incomplete conversions. Chemists in the field often mention improved yields or simply “reactions that go clean,” which, from repeated plant feedback, translates into easier downstream purification and better reproducibility.
Process chemists in pharmaceutical development often reach out with questions about product consistency, isomeric purity, and methods for scalable sulfonamide formation. Because of the precise substitution positions, this compound works well in designing drugs that need low background reactivity but high site selectivity for further functionalization. The –CF3 group, in particular, allows tuning of lipophilicity for harder-to-reach pharmacokinetic windows. Unlike generic sulfonyl chlorides, there’s less risk of unwanted byproduct accumulation—an insight shared by analysts reviewing hundreds of batch reports. Several APIs today trace critical steps to this material, making its reliable production more than just a technical goal but a direct contributor to medicine pipelines.
Agrichemical R&D teams have, over the years, reported that substituent-rich sulfonyl chlorides deliver pest and weed selectivity in new-generation control agents. On the manufacturing side, plant operators keep in mind that off-ratio impurities—often lower halogen content or incomplete trifluoromethylation—show up as performance drops at the field-testing stage. Manufacturing with controlled parameters doesn’t just supply the lab with base materials; it shapes outcomes in hundreds of hectares of cropland. Orders for this compound have grown alongside demands for safer, more targeted compounds with less environmental persistence.
Customers in regulated industries press for high specification documentation. From direct experience, reliable batches rarely drop below 98 percent GC purity, with strict controls on related substances. In-house HPLC and NMR equipment stays busy, comparing new lots against reference standards. Each analyst knows that downstream sulfonamide or sulfonate formation depends on eliminating isomeric and color-forming traces. Whenever an operator reports deviations, production halts for troubleshooting—a process learned from both regulatory audits and commonsense manufacturing discipline. A persistent belief on the floor: small sections of impurity in intermediates translate into waste elsewhere, so rigorous self-checks keep quality on track without heavy-handed corrective action from outside.
Handling 2,6-dichloro-4-(trifluoromethyl)benzenesulfonyl chloride day after day sharpens everyone’s awareness about environmental and occupational risks. Operators following chemical hygiene and batch protocols reduce the threat of releases to air or wastewater. Neutralization systems stand by for unexpected pressure or valve leaks, but consistent training typically prevents issues before escalation. Most waste captured during post-reaction workup undergoes neutralization and incineration under government-mandated procedures. These steps come from direct lessons: shortcuts show up as regulatory citations and, more importantly, real risks for those in proximity. Manufacturing teams often stress this culture on plant tours, highlighting that chemical innovation only matters when core safety is handled daily.
Not every synthetic route benefits from the presence of two chloro and one trifluoromethyl group. Teams in specialty material production sometimes find the advanced reactivity can derail multi-step sequences with intermediate incompatibilities, especially with nucleophilic or base-sensitive substrates. Lab-scale chemists might prefer a simpler sulfonyl chloride when side-reactions crop up, or when milder conditions suffice. From a production standpoint, the need for thoroughly clean reactors after every run slows scheduling in tight campaign environments. The material’s moisture sensitivity also rules out any casual storage in non-climate-controlled areas. These real limitations squeeze margins and timelines, so frequent coordination between process engineers and end users solves most bottlenecks.
Fulfilling demand for 2,6-dichloro-4-(trifluoromethyl)benzenesulfonyl chloride means keeping eyes open for shifts in global raw material pricing and availability. Producers in the field talk about early procurement of fluorinated intermediates to shield against force majeure events or market volatility. Transportation requires regulatory-compliant packaging plus real certificates of analysis per shipment. Teams in shipping and compliance remind everyone that even a single missing test result at a border can send back an entire lot, so tight record-keeping aligns with recognized best practices. Behind this, the entire production trace takes shape—from chlorination to bulk filling—delivering confidence when customs or regulatory agencies audit the trail.
Feedback from long-term customers who have run similar product suites brings recurring themes: 2,6-dichloro-4-(trifluoromethyl)benzenesulfonyl chloride delivers higher and faster conversion rates in sulfonamide synthesis than mono-substituted or unsubstituted analogs. For applications rolling out at kilogram scale, faster reaction eliminates repeated cycles and saves energy. Simpler aromatic sulfonyl chlorides occasionally outperform in stability or shelf life, but few match the selectivity and reduced byproduct profiles seen with this compound. Discussions with partners in the field show that while cost per kilogram sits higher, the savings on reaction time, purification burden, and batch uniformity easily offset the premium for process teams under tight time and quality constraints.
Innovating in production methods drives both higher quality and greater efficiency. Plant engineers routinely examine upgrades, such as process intensification or automation, that shrink reaction footprints without sacrificing safety. Lessons learned from pilot runs—like tweaking solvent ratios or optimizing drying conditions—move into full production thanks to open discussions among technical teams. Process improvement targets aren’t just about speed, but about minimizing off-spec residues and keeping energy use competitive. Investing in analytical tech pays off most on tight-margined products, where impurity profiles and reproducibility make the difference between a viable manufacturing business and a one-time production cycle.
Direct interactions with pharmaceutical and agrochemical sponsors bring home one truth: full transparency in QA processes builds trust in long-term partnerships. Maintaining traceable records, regular certificate audits, and robust change management stops supply disruptions before they begin. This material’s regulatory standing often draws lines around manufacturing practices, from validated cleaning processes to environmental controls set above minimum requirements. Observers on production tours regularly note how batch signoffs, raw material tracking, and result archiving run seamlessly, tracing every vial back to its origins. That rigor in everyday steps avoids import disputes and upholds customer confidence in both product and people.
Continued demand for tailored aromatic intermediates underscores the strategic importance of manufacturing compounds like 2,6-dichloro-4-(trifluoromethyl)benzenesulfonyl chloride. Teams working at the bench or in pilot plants explore expanded library synthesis, pushing to combine multiple substitutions to unlock new biological or materials properties. Expanding on-site capabilities, such as real-time process analytics or continuous flow chemistry, supports customers chasing aggressive project timelines. Every cycle through the plant reinforces a simple insight: depth in hands-on manufacturing, paired with responsiveness and validated performance, creates not just a product but a resource for advancing science and technology.
Facing the intricacies of producing and handling 2,6-dichloro-4-(trifluoromethyl)benzenesulfonyl chloride every day brings a perspective missed by those only reading spec sheets. Cost structure, batch consistency, and traceability depend on knowledge spread throughout the team—from process chemists to logistics coordinators. Decisions made in plant design, raw material selection, and risk management become visible in each shipment that reaches a customer’s bench. This compound keeps earning its place in demanding synthetic schemes because those producing it commit to every fine detail required for quality and safety. Chemical manufacturing rarely gives second chances for avoidable mistakes, and those who work with advanced intermediates like this one measure results by the smoothness of each campaign and the confidence of every returning customer.